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rs1085308012

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position22133586
GenePHEX
is asnp
is mentioned by
dbSNPrs1085308012
dbSNP (old)rs1085308012
ClinGenrs1085308012
ebirs1085308012
HLIrs1085308012
Exacrs1085308012
Gnomadrs1085308012
Varsomers1085308012
Maprs1085308012
PheGenIrs1085308012
Biobankrs1085308012
1000 genomesrs1085308012
hgdprs1085308012
ensemblrs1085308012
gopubmedrs1085308012
geneviewrs1085308012
scholarrs1085308012
googlers1085308012
pharmgkbrs1085308012
gwascentralrs1085308012
openSNPrs1085308012
23andMers1085308012
23andMe allrs1085308012
SNPshotrs1085308012
SNPdbers1085308012
MSV3drs1085308012
GWAS Ctlgrs1085308012
Max Magnitude0
ClinVar
Risk rs1085308012(C;C)
Alt rs1085308012(C;C)
Reference Rs1085308012(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22151703T>C
CLNSRC
CLNACC RCV000488975.1,